CN114315695B - Thermal activity delayed fluorescence molecular material based on indole condensed ring unit and application thereof - Google Patents

Thermal activity delayed fluorescence molecular material based on indole condensed ring unit and application thereof Download PDF

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CN114315695B
CN114315695B CN202111511647.7A CN202111511647A CN114315695B CN 114315695 B CN114315695 B CN 114315695B CN 202111511647 A CN202111511647 A CN 202111511647A CN 114315695 B CN114315695 B CN 114315695B
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CN114315695A (en
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税新凤
王亚飞
曹辰辉
庞玉东
李德宽
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Anhui Xiulang New Material Technology Co ltd
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Abstract

The application discloses a TADF molecular material based on indole condensed ring units. The application adopts two acceptor molecular structures based on indole condensed ring units, and modifies the two acceptor units based on indole condensed ring units. The application selects the derivatives of acridine and carbazole as donor molecules. Six target molecules M1-M6 are synthesized between the donor and the acceptor through Bachwald-hartwig coupling reaction, and the molecular structure of the target molecules is determined through nuclear magnetic resonance hydrogen spectrum or carbon spectrum.

Description

Thermal activity delayed fluorescence molecular material based on indole condensed ring unit and application thereof
Technical Field
The application relates to a preparation method of a thermal activity delayed fluorescence molecular material based on indole condensed ring units and application of the thermal activity delayed fluorescence molecular material in an electroluminescent device, belonging to the field of organic luminescent materials
Background
Organic Light-Emitting diodes (OLEDs) have been reported for the first time to now for more than thirty years with a continual improvement in new materials and device fabrication processes. This makes OLEDs not only widely used in people's life but also in military display technology. Wherein the display screen such as mobile phone, computer, digital camera, especially the television display technology field. OLED screens are evolving towards larger sizes, curved surfaces, richer and finer colors. However, there are problems with current organic light emitting diodes, such as: low luminous efficiency, short service life, high manufacturing cost and the like
For colorful organic electroluminescent materials, researchers can divide them into three-generation technical materials. The first generation of organic electroluminescent materials are the most traditional fluorescent materials, the utilization efficiency of the materials on singlet excitons is only 25% at most, the other three-quarter excitons are dissipated in a non-radiative transition mode, the actual luminous efficiency is about 6% at most, and the external quantum efficiency of the device is greatly limited to be improved due to the existence of the ceiling. In order to improve the luminous efficiency, the improvement of the utilization rate of excitons has become the focus of research by researchers, and phosphorescent materials have grown in a homeopathic manner. As a second generation fluorescent material, by introducing some heavy metal atoms having coordination ability into the molecule, the molecules utilize three-fourths of excitons which cannot be utilized in the first generation by utilizing the coupling action of spin orbitals, thereby achieving 100% exciton utilization. The material belongs to a third generation fluorescent material TADF (thermally activated delayed fluorescence) material, and under the condition of no noble metal doping, the material is thermally activated to enable the lowest triplet exciton to cross into the lowest singlet exciton through a reverse intersystem crossing, so that the 100% internal quantum efficiency is realized.
As the organic electroluminescent material which has been commercialized, the second generation phosphorescent material has many problems in that the phosphorescent material needs to use expensive noble metal (iridium, platinum) complexes, is not only economically expensive, but also pollutes the environment, and cannot be environmentally friendly, so that the economical and environmental costs of the phosphorescent material are high. In addition, the phosphorescent material can stabilize blue luminescence, has few material types and lower service life, and can not fully meet the commercialization requirement. The TADF molecular material used as the third-generation fluorescent material can make up for the defects to a certain extent, and is worthy of research by researchers as an emerging fluorescent material with potential and application value.
Disclosure of Invention
The application provides a TADF molecular material based on indole condensed ring units, which is characterized in that: the donor group with electron donating ability in the molecule is carbazole derivative and acridine derivative, the acceptor group with electron withdrawing ability is indole condensed ring unit, and the characteristic structure is as follows:
the application also provides application of the TADF molecular material based on the indole condensed ring unit in an electroluminescent device, which is characterized in that: the organic light-emitting layer in the electroluminescent device is made of the TADF molecular material.
The beneficial effects are that:
according to the luminescence mechanism of thermally active delayed fluorescence materials, the acquisition of Delayed Fluorescence (DF) has two important processes, the first one is T 1 -S 1 In an effort to achieve lower ΔE in RISC (reverse inter-line cross-over) process st Both (triplet exciton to singlet exciton energy difference) and thermally-active delayed fluorescence molecule HOMO to LUMO separation promote intra-molecular ICT in favor of improved molecular related properties. The second important process is S 1 -S 0 The high fluorescence quantum yield in this process is advantageous for improving the molecular-related properties. In order to make the material more efficient, it is often necessary to select the appropriate donor and acceptor and linkage to achieve separation of HOMO from LUMO.
The Thermally Active Delayed Fluorescence (TADF) molecular material based on indole fused ring units of the application is as follows: generally, the molecules based on aromatic condensed rings or hetero-atom aromatic condensed rings have stronger electron withdrawing capability, so that two acceptor molecular structures based on indole condensed ring units, namely an aromatic condensed ring acceptor based on indole condensed ring units and a heteroaromatic condensed ring acceptor containing an indole condensed ring unit with nitrogen hetero atoms are designed and synthesized in the application; carbazole/acridine derivative donor units are introduced into the peripheries of the two condensed ring units based on indole, so that the intramolecular charge transfer effect of molecules is increased, and the HOMO and LUMO of the molecules are separated; on the other hand, the indole condensed ring unit improves the rigid structure of the molecule, inhibits the non-radiative transition of the molecule, and improves the luminous efficiency of the material; the carbazole derivative-3, 6-di-tert-butylcarbazole has the advantages of very high bond-off energy, good rigid conjugated plane, good electron donating ability and the like, and is favorable for constructing efficient and stable luminescent materials. Therefore, the application uses indole condensed ring unit with rigid structure as receptor, and can obtain high-efficiency red light TADF luminescent material by changing the receptor-donating structure of molecule.
Drawings
FIG. 1 shows the preparation of Compound M according to one embodiment of the present application 1 -M 6 TGA profile of (c).
FIG. 2 shows the preparation of Compound M according to one embodiment of the present application 1 -M 6 Is a CV curve of (c).
FIG. 3 shows the preparation of Compound M according to one embodiment of the present application 1 -M 3 A molecular Density Functional Theory (DFT) calculation curve.
FIG. 4 shows the preparation of Compound M according to one embodiment of the present application 4 -M 6 A molecular Density Functional Theory (DFT) calculation curve.
FIG. 5 shows the preparation of Compound M according to one embodiment of the present application 1 -M 6 Ultraviolet absorption and photoluminescence curves in toluene solutions.
FIG. 6 shows the preparation of Compound M according to one embodiment of the present application 1 -M 6 The luminous intensity of the oxygen removal and the non-oxygen removal is briefly compared with each other.
FIG. 7 shows the preparation of Compound M according to one embodiment of the present application 1 -M 3 The EL spectra (left) and the J-V-L curves (right) of the device at 10wt%, 15wt%, 20wt% doping.
FIG. 8 shows the preparation of Compound M according to one embodiment of the present application 4 -M 6 The EL spectrum (left) and the J-V-L curve (right) of the device under doping of 1wt%, 3wt%, 5wt%.
FIG. 9 shows the preparation of Compound M according to one embodiment of the present application 1 -M 3 The EQE curves for 10wt%, 15wt%, 20wt% doped devices.
FIG. 10 shows the preparation of Compound M according to one embodiment of the present application 4 -M 6 The EQE curves of the devices under 1wt%, 3wt%, 5wt% doping.
FIG. 11 shows the preparation of Compound M according to one embodiment of the present application 1 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
FIG. 12 shows the preparation of Compound M according to one embodiment of the present application 2 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
FIG. 13 shows the preparation of Compound M according to one embodiment of the present application 3 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
FIG. 14 shows the preparation of Compound M according to one embodiment of the present application 4 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
FIG. 15 shows the preparation of Compound M according to one embodiment of the present application 5 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
FIG. 16 shows the preparation of Compound M according to one embodiment of the present application 6 A kind of electronic device 1 H NMR(400MHz,CDCl 3 ) Nuclear magnetic resonance hydrogen spectrum.
Detailed Description
The present application is further illustrated below in conjunction with specific embodiments, it being understood that these embodiments are meant to be illustrative of the application and not limiting the scope of the application, and that modifications of the application, which are equivalent to those skilled in the art to which the application pertains, fall within the scope of the application as defined in the appended claims after reading the application.
Example 1
The application M 1 、M 2 The target molecule can be synthesized according to the following reaction scheme:
synthesis of Compound 2
The 1, 4-dioxane is dried by sodium block reflux, and can be distilled out for use after being changed into dark blue after being added with benzophenone. 1, 4-Dibromobenzene (9.40 g,40 mmol), bis (pinacolato) diboron (25.39 g,100 mmol), potassium acetate (9.81 g,100 mmol) were added to a three-necked flask, the dried 1, 4-dioxane was added, and finally [1,1' -bis (diphenylphosphino) ferrocene was added]DichlorinationAfter palladium (1.46 g,2 mmol), the reaction system was sealed and replaced with nitrogen and refluxed overnight under nitrogen protection. The reaction was terminated by opening the seal and adding an appropriate amount of distilled water. Extracting with appropriate amount of dichloromethane three times, mixing organic phases, and washing with appropriate amount of distilled water three times. The organic phase was dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness under reduced pressure. Purifying the crude product by silica gel column chromatography, wherein the eluent is dichloromethane: petroleum ether = 1:4 to give a white powder solid in 82% yield. 1 H NMR(400MHz,CDCl3)δ7.80(s,4H),1.35(s,24H).
Synthesis of Compound 3
1, 4-Diphenyl-boronic acid pinacol ester (1 g,3 mmol), methyl 2-iodo-5-bromo-benzoate (2.25 g,6.6 mmol), was first added to a three-necked flask, potassium carbonate (2.49 g,18 mmol) was added as a 2mol/L aqueous solution, and tetrakis (triphenylphosphine) palladium (173 mg,0.15 mmol) was finally added to the reaction three-necked flask. The volume ratio of toluene to ethanol is 3:1 as solvent, nitrogen is replaced three times and the reaction is carried out at 85 ℃ overnight under the protection of nitrogen. Cooling to room temperature, evaporating under reduced pressure, extracting with dichloro three times while washing with water three times, mixing organic phases, drying over anhydrous magnesium sulfate, filtering, evaporating under reduced pressure, and drying. Purifying the crude product by silica gel column chromatography, wherein the eluent is dichloromethane: petroleum ether = 1:4 to give a white yellowish powder solid in 52% yield. 1 H NMR(400MHz,CDCl3)δ7.98(d,J＝2.0Hz,1H),7.67(dd,J＝8.2,2.0Hz,1H),7.31(t,J＝3.8Hz,3H),3.69(s,3H).
Synthesis of Compound 4
Distilled water and concentrated sulfuric acid (the concentration is 99.99%) are prepared into 80% concentrated sulfuric acid according to the volume ratio of 1:4, and the concentrated sulfuric acid is cooled to room temperature for standby. Compound 3 (1 g,2 mmol) was added to 100ml of 80% concentrated sulfuric acid and reacted at 120℃for 9 to 10 hours, and as the reaction proceeded, the starting material changed from a white yellowish solid to a dark reddish black solid. And cooling the reaction system to room temperature, and slowly pouring the reaction system into ice cubes until the residual ice cubes in the reaction liquid are not heated any more. Finally, the mixture is decompressed and filtered, washed three times by methanol and petroleum ether and dried at 65 ℃ to obtain red-black solid with the yield of 87 percent. Since this compound is substantially insoluble in common solvents, the crude product is no longer furtherPurified and used directly in the next step. Compound 4 had poor solubility in the commonly used deuterated reagents, giving a crude hydrogen profile. 1 H NMR(400MHz,DMSO)δ8.08(s,1H),7.85(s,2H),7.74(s,1H).
Target compound M 1 Synthesis of (IndoPh-DBuCz)
And (3) refluxing and drying toluene by using sodium blocks, and adding benzophenone to turn deep blue and then evaporating the toluene for use. Firstly, compound 4 (1.00 g,2.27 mmol), 3, 6-di-tert-butylcarbazole (1.52 g,5.46 mmol) and sodium tert-butoxide (1.09 g,11.36 mmol) are added into a three-mouth bottle, dried toluene is taken out and added into a reaction system, after stirring for 10min at room temperature, tris (dibenzylideneandene acetone) dipalladium (124 mg,0.12 mmol) is added, the reaction system is sealed, nitrogen is replaced three times, toluene solution containing tri-tert-butylphosphine (97mg0.48 mmol) is injected under the protection of nitrogen, and the mixture is placed at 110 ℃ for reaction overnight. After the reaction was terminated by opening the seal, it was distilled to dryness under reduced pressure, extracted three times with methylene chloride and washed three times with water, and the organic phases were combined, dried over anhydrous magnesium sulfate, filtered, and distilled to dryness under reduced pressure. Purifying the crude product by silica gel column chromatography, wherein the eluent is dichloromethane: petroleum ether = 1:2.5 to give a violet powder solid in 68% yield. The nuclear magnetic resonance results are shown in FIG. 11.
1 H NMR(400MHz,CDCl3)δ8.15(s,1H),7.94(s,1H),7.79(s,1H),7.50(d,J＝7.9Hz,1H),7.40(d,J＝8.6Hz,1H),1.48(s,9H).
13 C NMR(101MHz,CDCl 3 )δ143.63,141.34,139.84,138.68,135.76,132.74,129.05,128.24,123.93,123.81,122.53,121.97,116.47,116.31,109.22,34.80,31.99.
MALDI-MS(m/z)of C 60 H 56 N 2 O 2 for[M + ]:calcd.836.43；found,836.47
Target compound M 2 Synthesis of (IndoPh-DMeAd)
And (3) refluxing and drying toluene by using sodium blocks, and adding benzophenone to turn deep blue and then evaporating the toluene for use. First, compound 4 (1.00 g,2.27 mmol), 9, 10-dihydro-9, 9-dimethylacridine (1.14 g,5.46 mmol) and sodium t-butoxide (1.09 g,11.36 mmol) were added to a three-necked flask, dried toluene was taken out, the reaction system was stirred at room temperature for 10min, then the reaction system was sealed after adding tris (dibenzylideneandene acetone) dipalladium (124 mg,0.12 mmol), nitrogen was replaced three times, and a toluene solution containing tri-t-butylphosphine (97 mg,0.48 mmol) was injected under nitrogen protection and reacted at 110℃overnight. After the reaction was terminated by opening the seal, it was distilled to dryness under reduced pressure, extracted three times with methylene chloride and washed three times with water, and the organic phases were combined, dried over anhydrous magnesium sulfate, filtered, and distilled to dryness under reduced pressure. Purifying the crude product by silica gel column chromatography, wherein the eluent is dichloromethane: petroleum ether = 1:2.5 to give a violet powder solid in 34% yield. The nuclear magnetic resonance results are shown in FIG. 12.
1 H NMR(400MHz,CDCl3)δ7.97(s,1H),7.86(d,J＝7.8Hz,1H),7.73(s,1H),7.59(d,J＝7.7Hz,1H),7.49(d,J＝7.4Hz,2H),7.26(s,2H),7.11–6.92(m,4H),6.38(d,J＝7.9Hz,2H),1.70(s,6H).
13 C NMR(101MHz,CDCl 3 )δ191.41,145.55,143.02,142.93,140.43,140.02,139.59,138.79,138.69,137.89,136.81,135.49,130.51,130.47,129.75,129.05,128.24,128.14,128.04,126.50,125.45,125.41,125.31,124.70,123.01,122.84,121.17,121.13,120.82,116.58,116.32,116.28,113.97,36.05,31.10,29.71,21.46.
The application M 3 The target molecule can be synthesized according to the following reaction scheme:
synthesis of Compound 9
Adding a proper amount of calcium hydride into the dichloromethane solution, refluxing and drying the mixture, and taking the mixture. Aluminum trichloride (9.33 g,70 mmol) and methylene chloride (200 ml) taken after the above drying were placed in a three-necked flask, and 3-chloropropionyl chloride (8.89 g,70 mmol) and methylene chloride (50 ml) taken after the above drying were placedThe solution was slowly dropped into a dichloromethane solution containing aluminum trichloride in a constant pressure dropping funnel. After the completion of the dropwise addition, the mixture was stirred at 25℃for 20 minutes. Bromobenzene (9.89 g,63 mmol) was dissolved in dichloromethane (10 ml) and placed in a constant pressure dropping funnel, and the above reaction system was slowly added dropwise, and reacted overnight at 25℃after the completion of the dropwise addition. After the reaction was completed, a 2M diluted hydrochloric acid solution was prepared and cooled with an ice water bath, then the reaction solution was slowly poured into an ice 2M diluted hydrochloric acid solution, the organic phase was combined by extraction with methylene chloride three times and washed three times with saturated sodium bicarbonate, and after drying by adding anhydrous magnesium sulfate into the organic phase, the mixture was evaporated to dryness under reduced pressure. The product was white and yellowish, which was a solid at room temperature, and was dissolved after slightly heating, with a yield of 98%. The crude product obtained above is not further purified and is directly put into the next step for use. 1H NMR (400 MHz, CDCl) 3 )δ7.87–7.77(m,2H),7.63(dd,J＝8.5,1.4Hz,2H),3.91(t,J＝6.8Hz,2H),3.43(t,J＝6.8Hz,2H).
Synthesis of Compound 10
4-bromo-benzoylethyl chloride (6.39 g,28.83 mmol) was added to a three-necked flask, reacted with concentrated sulfuric acid (100 ml) as a solvent at 120℃for 120min, and cooled to room temperature. Pouring the reaction system into ice for dilution and cooling, extracting with methylene dichloride for three times after cooling to room temperature, merging organic phases, washing the organic phases with saturated sodium bicarbonate for two times, washing the organic phases with distilled water for one time, metering anhydrous magnesium sulfate into the organic phases, filtering, and performing rotary evaporation under reduced pressure until the organic phases are dry. Purifying the crude product by silica gel column chromatography, wherein the eluent is dichloromethane: petroleum ether = 1:2.5 to give a violet powder solid in 56% yield. 1H NMR (400 MHz, CDCl 3) delta 7.64 (s, 1H), 7.59 (d, J=8.1 Hz, 1H), 7.49 (d, J=8.1 Hz, 1H), 3.19-3.06 (m, 2H), 2.80-2.60 (m, 2H).
Synthesis of Compound 12
Adding 9.94g of 5-bromo-1-indanone (47.1 mmol) into a three-necked flask containing 250ml of pure benzene, acidifying 6.11g of isoamyl nitrite (52.14 mmol) with 20ml of concentrated hydrochloric acid, placing into a constant pressure dropping funnel, slowly dropwise adding the mixture into the three-necked flask containing 5-bromo-1-indanone and pure benzene at 40 ℃, gradually precipitating white precipitate in the dropwise adding process, reacting for 3h after the dropwise adding, and reacting for three times at room temperature (25 ℃)And (3) days. The reaction system becomes a solid-liquid mixed system after three days, the reaction system is decompressed and filtered to obtain a white yellowish solid filter cake, and the filter cake is respectively washed by a proper amount of methanol and diethyl ether and then is dried in a drying oven at 60 ℃. A white powder solid was obtained in 82% yield. 1 H NMR(400MHz,CDCl3)δ7.78(d,J＝8.1Hz,1H),7.70–7.60(m,2H),4.03(s,2H).
Synthesis of Compound 13
Sodium dithionite 4.5g 18.75mmol and 5-bromo-2-nitroso-1-indanone 9.8g 56.25mmol are placed in a 250ml round bottom flask and 45ml ethanol is added and stirred under nitrogen to form a suspension. 20ml of 25% -28% ammonia water was injected into the round bottom flask, and 18ml of distilled water was injected. The reaction was carried out at 25℃for three days, and the reaction system was changed from white to yellow-red as the reaction proceeded while the suspension became thick. After three days of reaction, the reaction system was divided into two parts, which were respectively put into two 250ml round bottom flasks, and 23ml distilled water was respectively added to reflux for 24 hours. After stopping heating, the reaction system was cooled to room temperature, 45ml of distilled water was added to each of the two round-bottomed flasks and stirred for 1 hour, and a yellow cake was obtained after filtration, which was washed with methanol and then diethyl ether, and dried at 60℃to give a yellow solid (2.44 g 63%).
1 H NMR(400MHz,CDCl 3 )δ8.01(dd,J＝33.3,8.3Hz,1H),7.80(s,1H),7.65(d,J＝8.3Hz,1H),4.04(d,J＝13.0Hz,2H).
Synthesis of Compound 14
2, 8-dibromo-6, 12-dihydro-diindeno [1,2-b:1,2-e]Pyrazine (2 g,4.8 mmol), sodium dichromate dihydrate (4.29 g,14.4 mmol), acetic acid 160ml and acetic anhydride 18ml were added sequentially to a 500ml round bottom flask and reacted at 120℃for 24h under nitrogen. The color of the reaction system gradually changed from orange to red as the reaction proceeded. The reaction system was cooled to room temperature, and 160ml of distilled water was continuously added, stirred for 10min, and suction filtration was performed to obtain a red cake, and then the cake was washed with an appropriate amount of methanol and diethyl ether, and dried at 60 ℃ to obtain 1.55g of a red solid, 73.2%. The compound has extremely poor solubility in common deuterated reagents, 1 H NMR(400MHz,CDCl3)δ7.98(s,1H),7.89(s,2H).
target compound M 3 Synthesis of (IndoPy-DBuCz)
Toluene was dried with sodium block, and after adding benzophenone solution to turn deep blue, distilled to get it. 2, 8-dibromo-6, 12-dione-diindeno [1,2-b:1,2-e ] pyrazine (1 g,2.26 mmol), 3, 6-di-tert-butylcarbazole (1.52 g,5.42 mmol), sodium tert-butoxide (1.09 g,11.30 mmol), dried toluene 50ml, tris dibenzylideneacetone dipalladium (110 mg,0.12 mmol) was added to a 100ml round bottom flask and the mixture was reacted under nitrogen with tri-tert-butylphosphine (1.8 ml of 0.1M toluene solution, 0.18 mmol) at 110℃for 12h. After cooling to room temperature, toluene was distilled off under reduced pressure, extracted with methylene chloride, washed with distilled water and distilled to dryness to give a crude product. Purification by column chromatography on silica gel (eluent: dichloromethane) and drying at 60℃gave a yellow solid (0.66 g, 34.81%) as a result of nuclear magnetism, see FIG. 13.
1 H NMR(400MHz,CDCl3)8.23(d,J＝8.0Hz,1H),8.15(s,2H),8.11(d,J＝1.7Hz,1H),7.96(dd,J＝7.9,1.8Hz,1H),7.52(dd,J＝8.6,1.6Hz,2H),7.46(d,J＝8.6Hz,2H),1.48(s,18H).
13 C NMR(101MHz,CDCl 3 )δ188.66,160.38,149.88,144.20,142.35,138.30,137.58,135.53,133.51,129.04,128.23,125.30,124.16,124.13,123.80,122.19,116.58,109.29,34.83,31.96,21.45.
The application M 4 The target molecule can be synthesized according to the following reaction scheme:
target compound M 4 Synthesis of (IndoPh-DBuCz-CN)
Compound M 1 (800 mg,0.96 mmol) of solid was first added to a round bottom flask, dried chlorobenzene was added as a solvent for the reaction, and malononitrile (951 mg,14.4 mmol) titanium tetrachloride (1821 mg,9.6 mmol) and pyridine (1519 mg,19.2 mmol) were all injected into the reaction system by means of syringe weighing, reacted at 110℃for 5 hours, cooled to room temperature and quenched with an appropriate amount of water, and then distilled under reduced pressure to dryness to give a crude product. Make the following stepsPurification by column chromatography on silica gel (eluent: dichloromethane) was dried at 60℃to give 286.72mg of yellow solid in 32.0% yield. The nuclear magnetic resonance results are shown in FIG. 14.
1 H NMR(400MHz,CDCl3)δ8.69(d,J＝3.1Hz,2H),8.15(s,2H),7.89(d,J＝8.2Hz,1H),7.81(d,J＝9.0Hz,1H),7.72(d,J＝3.3Hz,1H),7.52(t,J＝8.8Hz,5H),7.42(d,J＝8.5Hz,2H),7.35(s,2H),7.18–6.95(m,4H),1.56–1.35(m,36H).
MALDI-MS(m/z)of C 66 H 56 N 6 for[M + ]:calcd.932.46；found,932.88
The application M 5 The target molecule can be synthesized according to the following reaction scheme:
target compound M 5 Synthesis of (IndoPh-DMEAd-CN)
Compound M 2 (700 mg,1 mmol) of the solid was first added to a round-bottomed flask, dried chlorobenzene was added as a solvent for the reaction, nitrogen was used as a protection, and malononitrile (990 mg,15.0 mmol) titanium tetrachloride (1896.8 mg,10.0 mmol) and pyridine (1582 mg,20 mmol) were all injected into the reaction system by weighing them by means of a syringe, reacted at 110℃for 5 hours, the reaction system was cooled to room temperature and quenched with an appropriate amount of water, and then distilled under reduced pressure to dryness to give a crude product. Purification was performed by column chromatography on silica gel (eluent: dichloromethane) and dried at 60℃to give 449.5mg of a red solid in a yield of 56.4%. The nuclear magnetic resonance results are shown in FIG. 15.
1 HNMR(400MHz,CDCl 3 8.75(s,1H),8.42(s,1H),7.98(d,J＝7.9Hz,1H),7.64(d,J＝7.9Hz,1H),7.51(d,J＝6.9Hz,2H),7.01(p,J＝7.0Hz,4H),6.35(d,J＝7.8Hz,2H),1.72(s,6H).
13 C NMR(101MHz,CDCl 3 )δ158.49,143.43,142.91,140.39,140.33,139.64,139.29,136.86,130.72,130.51,126.57,125.70,123.47,121.42,118.71,113.93,112.96,112.40,36.09,31.23.
The application M 6 The target molecule may be synthesized according to the following reaction,the specific reaction route is as follows:
target compound M 6 (IndoPy-DBuCz-CN)
Compound M 3 (600 mg,0.72 mmol) was directly added to a round-bottomed flask, dried chlorobenzene was used as a solvent, malononitrile (719 mg,10.8 mmol) titanium tetrachloride (1366 mg,7.2 mmol) pyridine (1139 mg,14.4 mmol) was injected into the round-bottomed flask by weighing with a syringe, nitrogen protection was applied at 110℃for 5h, the reaction system was cooled to room temperature, and distilled under reduced pressure to dryness to give a crude product. Purification was by column chromatography on silica gel (eluent: dichloromethane) and oven-dried at 60deg.C to give 159.5mg of a yellow solid in 23.7% yield. The nuclear magnetic resonance results are shown in FIG. 16.
1 H NMR(400MHz,CDCl3)δ8.77(s,1H),8.23(d,J＝7.9Hz,1H),8.15(s,2H),7.95(s,1H),7.51(s,2H),7.48(s,2H),1.48(s,18H).
Example 2
The thermal stability of the target compound was tested by thermogravimetric analysis (TGA).
In the test, the weight of the sample is 2-5mg, the system is protected by nitrogen, the temperature is raised from room temperature to 600 ℃ at the speed of 20 ℃/min, the TGA curve is tested, and the temperature corresponding to the weight loss of 5% is defined as the thermal decomposition temperature (T) d ). As shown in FIG. 1, the target compound M 1 (Indo-Ph-DBuCz)、M 2 (Indo-Ph-DMeAd)、M 3 The thermal decomposition temperatures (loss of 5% by weight) of (Indo-Py-DBuCz) were 495, 427, 467 ℃. Wherein M is 1 (Indo-Ph-DBuCz) has a stronger rigid structure and a higher total bond energy, and therefore its decomposition temperature is higher than the other two materials. M is M 3 (Indo-Py-DBuCz) the total bond energy is slightly reduced due to the introduction of heteroatoms, M 3 (Indo-Py-DBuCz) thermal decomposition temperature (T d ) Slightly smaller than M 1 (Indo-Ph-DBuCz)；M 4 :Indo-Ph-DBuCzCN、M 5 :Indo-Ph-DMeAdCN、M 6 The thermal decomposition temperatures (loss of 5% by weight) of Indo-Py-DBuCzCN were 392, 415, 473℃respectively. The introduction of the cyano group forms a carbon-carbon double bond,M 4 、M 5 、M 6 and M is as follows 1 、M 2 、M 3 The thermal decomposition temperatures are slightly reduced in one-to-one correspondence. M is M 4 、M 5 、M 6 M in (v) 4 (Indo-Ph-DBuCzCN) and M 5 (Indo-Ph-DMeAdCN)、M 6 (Indo-Py-DBuCzCN) has a stronger rigid structure and a higher total bond energy than the other two target compounds, and therefore its decomposition temperature is higher than that of the other two target compounds. The important significance of analyzing the TGA curve is that the thermal decomposition temperatures of the three materials are large, the three materials have good thermal properties, and the requirements of the organic electroluminescent device can be met.
Example 3
CV curve of test target molecule
The specific implementation method is as follows: cyclic Voltammetry (CV) curves were tested by the CHI-660A electrochemical workstation. Under the protection of nitrogen, the platinum plate electrode and the platinum wire electrode are respectively a working electrode and a counter electrode, the metal silver and the silver chloride (Ag/Ag Cl) are used as reference electrodes, and ferrocene (Fc/Fc) + ) As an internal standard, 0.1mol/L tetrabutylammonium hexafluorophosphate (Bu 4 NPF 6 ) The acetonitrile of (2) is used as electrolyte, a sample is prepared into a chloroform solution, and the chloroform solution is coated on a working electrode for testing to obtain a CV curve of target molecules.
Compound M as shown in FIG. 2 1 、M 2 、M 3 Exhibits an irreversible oxidation-reduction potential in the range of-1.5 to 2.0V, and exhibits a redox potential (E ox ) And reduction potential (E) red ) The value is represented by the formula:
E (HOMO) (eV)＝－(E ox.vsFc/Fc+ +4.8)eV；
E (LUMO) (eV)＝－(E red.vsFc/Fc+ +4.8)eV；
E ox.vsFc/Fc+ ＝(E ox －E label (C) )eV，E red.vsFc/Fc+ ＝(E red －E Label (C) )eV；
Calculated to obtain M 1 ～M 3 The HOMO levels of (C) are-4.26, -4.82, -4.81eV, respectively, and the LUMO levels are-2.83, -2.90, -2.88eV, respectively. M is M 1 And M is as follows 3 The analysis results can be obtained by introducing aza-sourceThe electrons have a larger influence on the HOMO level and a smaller influence on the LUMO level.
Calculated to obtain M 4 、M 5 、M 6 The HOMO levels of (C) are-4.28, -4.58, -3.9eV, respectively, and the LUMO levels are-2.88, -3.10, -2.75eV, respectively. M is M 4 And M is as follows 6 The analysis results show that the introduced nitrogen heteroatom has a larger influence on the HOMO energy level and a smaller influence on the LUMO energy level.
Example 4
Density Functional Theory (DFT) calculation of target compounds
This M was done using Gaussian 09 program 1 ～M 6 Density Functional Theory (DFT) calculations. As shown in FIG. 3 and FIG. 4, the molecular Density Functional Theory (DFT) calculation result shows that M 1 The HOMO of the molecule is predominantly distributed over carbazole units within the molecule, with a small distribution of acceptor cores. Its LUMO is mainly concentrated on the acceptor core; m is M 2 The molecular Density Functional Theory (DFT) calculation results indicate M 2 The HOMO of the molecule is predominantly distributed on donor acridine units within the molecule, with a relatively concentrated distribution. Its LUMO is mainly concentrated on the acceptor core; m is M 3 The molecular Density Functional Theory (DFT) calculation results indicate M 3 The HOMO of the molecule is predominantly distributed over carbazole units within the molecule, with a small distribution of acceptor cores. Its LUMO is mainly concentrated on the acceptor core.
M can be seen by comparing the three molecules with each other 1 And M is as follows 3 There is some cross-distribution in the spatial separation of HOMO and LUMO distributions. M is M 3 Molecule and M 1 Molecular comparison, M 3 The introduction of the molecular acceptor core N heteroatom slightly promotes the separation of HOMO from LUMO of the molecule. And M is 2 The LUMO and HOMO distributions of the molecules overlap minimally, the spatial separation is better, and the intersystem crossing of triplet excitons is most effectively promoted. To sum up M 2 Molecules are the most sterically efficient separated molecules of LUMO and HOMO.
M 4 The molecular Density Functional Theory (DFT) calculation results indicate M 4 The HOMO of the molecule is predominantly distributed over carbazole units within the molecule, with a small distribution of acceptor cores. Its LUMO is mainly concentrated inA receptor core; m is M 5 The molecular Density Functional Theory (DFT) calculation results indicate M 5 The HOMO of the molecule is predominantly distributed on donor acridine units within the molecule, with a relatively concentrated distribution. Its LUMO is mainly concentrated on the acceptor core; m is M 6 The molecular Density Functional Theory (DFT) calculation results indicate M 6 The HOMO of the molecule is predominantly distributed over carbazole units within the molecule, with a small distribution of acceptor cores. Its LUMO is mainly concentrated on the acceptor core.
M can be seen by comparing the three molecules with each other 4 And M is as follows 6 There are some cross-separation imperfections in the spatial separation of HOMO and LUMO distributions. And M is 5 The LUMO and HOMO distributions of the molecules overlap minimally, the spatial separation is better, and the intersystem crossing of triplet excitons is most effectively promoted. In conclusion, the M5 molecule is the most spatially separated molecule of LUMO and HOMO, and the relevant OLED performance is probably the best of these three molecules.
Example 5
The specific implementation method is as follows: the ultraviolet-visible absorption spectrum (UV-vis) is obtained by measuring the target compound (10) with a CARY100 type ultraviolet-visible spectrophotometer of Agilent corporation -5 M) toluene solution test. Test of target compounds by Edinburgh FLS980 was performed in the presence of oxygen scavenging (10 -5 M) photoluminescence spectrum in toluene.
As shown in FIG. 5 (left), it is compound M 1 ～M 6 In toluene solution (10) -5 M) an ultraviolet visible absorption spectrum and a photoluminescence spectrum. As can be seen from FIGS. 2-7, M 1 And M is as follows 3 Is similar to the ultraviolet absorption peak type, and the nitrogen atom is introduced to lead M 3 The ultraviolet absorption of the molecules moves towards shortwaves. Compound M 1 ～M 3 Absorption peaks in the 300-350nm range are mainly ascribed to pi-pi of the intramolecular aromatic ring * A transition; the broad absorption peak between 350-500nm is the charge transfer transition (ICT) of the intramolecular donor unit to the acceptor unit.
M 4 And M is as follows 6 Similarly to the ultraviolet absorption peak type, and likewise, the nitrogen atom is introduced so that M 6 The ultraviolet absorption of the molecules moves towards shortwaves. Compound M 4 ～M 6 In the 300-350nm regionThe absorption peak between the two is mainly attributed to pi-pi of the aromatic ring in the molecule * A transition; the broad absorption peak between 350-500nm is the charge transfer transition (ICT) of the intramolecular donor unit to the acceptor unit.
M 1 ～M 6 The maximum emission peaks obtainable by photoluminescence spectra were 621nm, 641nm, 622nm, 681nm, 622nm, respectively.
Example 6
As shown in FIG. 6M 1 ～M 6 Toluene solution (10) with (up) and without (down) oxygen removal -5 M) photoluminescence intensity shorthand comparison. Oxygen molecules can quench triplet excitons effectively, while less influence on singlet emission in order to study delayed fluorescence characteristics of three materials, PL spectra of them in toluene solution under room temperature condition were tested under nitrogen deoxygenated solution and solution condition exposed to air, and then fluorescence intensity was compared with M 1 ～M 6 The fluorescence intensity is slightly enhanced under the condition of nitrogen deoxidizing solution, which shows that oxygen quenches triplet excitons in air, inhibits RISC process, and further shows that M is provided 4 ～M 6 Has delayed fluorescence characteristic.
Example 7
The embodiment of the application provides a method based on the six M 1 ～M 6 The specific preparation method of the organic electroluminescent device prepared by the novel TADF molecule comprises the following steps:
in the form of compound M 1 ～M 3 The light-emitting layer dopant is prepared by taking CBP as a main material and adopting a solution spin coating method. Wherein Compound M 1 ～M 3 The doping ratio of (2) is 10wt%, 15wt% and 20wt%. The specific device structure is as follows:
ITO/PEDOT PSS (40 nm)/EML (10 nm)/TmPyPB (45 nm)/LiF (0.5 nm)/Al (120 nm), wherein ITO is an anode, PEDOT PPS is a hole transport layer CBP and is a host doping material, emitter is a guest luminescent material, tmPyPB is an electron transport layer, and LiF/Al is a cathode.
In the form of compound M 4 ～M 6 The light-emitting layer dopant is prepared by taking PVK: OXD-7 (7:3) as a main material and adopting a solution spin coating method.Wherein Compound M 4 ～M 6 The doping ratio of (2) is 1wt%, 3wt% and 5wt%. The specific device structure is as follows:
ITO/PEDOT: PSS (40 nm)/PVK: OXD-7 (7:3): xwt% dopant (50 nm)/TmPyPB (45 nm)/LiF (0.5 nm)/Al (100 nm). Wherein ITO is an anode, PEDOT: PPS is a hole transport layer PVK: OXD-7 (7:3) is a host doping material, emitter is a guest light emitting material, tmPyPB is an electron transport layer, and LiF/Al is a cathode.
Example 8
The application provides six molecules M 1 ～M 6 EL spectrum and J-V-L of the device. As shown in FIG. 7 (left) and FIG. 8 (left) is M 1 ～M 3 Electroluminescent spectrum of device. From the figure, their EL spectra exhibited a single emission peak. Emission peaks around 400nm originate from the luminescence of the host material CPB and are of great intensity, which suggests that the energy transfer between host and guest materials is incomplete, and finding a suitable host material to enable better energy matching is a major problem at present. The emission of the long wave around 700nm is M 1 ～M 3 The material emits light. Experimental results indicate that M 1 The best performance is achieved at 20wt% doping (Ph-Cz 20%). M is M 2 The best performance is achieved at 20wt% doping (Ph-Ac 20%). M is M 3 The best performance is achieved at 20wt% doping (qin-Cz 20%). M is M 4 ～M 6 The device has an emission peak of 450nm at the doping ratio of 1wt%, 3wt% and 5wt%, and is derived from the host material PVK, OXD-7 (7:3), and has high intensity. M is M 4 The device has very small emission peaks at doping ratios of 1wt%, 3wt% and 5wt%. This illustrates that little energy transfer between host and guest materials, finding a suitable host material to enable better energy matching is currently a major problem.
The J-V-L curves shown in FIG. 7 (right), FIG. 8 (right) can be obtained: m is M 1 The material has a maximum brightness of 85.82cd/m at 10wt% doping 2 ；M 2 The material has a maximum luminance of 101.6cd/m at 10wt% doping 2 M 1 The highest brightness of the material under the doping of 10 weight percent is 55.71cd/m 2 。 .
M is obtained from the J-V-L curves shown in FIGS. 3-9 4 ～M 6 The maximum brightness of the device is 61.97, 9.51 and 83.36cd/m respectively under the doping proportion of 1wt%, 3wt% and 5wt% 2 。
Example 9
The application provides six molecules M 1 ～M 6 The EQE curve of the device of (a). As shown in FIG. 9, is compound M 1 ～M 3 The doping proportion of the light-emitting layer dopant is 10wt%, 15wt% and 20wt% of the EQE of the device. M is M 1 ～M 3 M in molecule 2 The best EQE is shown. Overall M 1 ～M 3 The device exhibits lower external quantum efficiency at 10wt%, 15wt%, 20wt% doping. M is M 1 ～M 3 Poor solubility of molecules and M 1 ～M 3 Mismatch of device host material guest material is a significant cause of device inefficiency. If the two problems can be improved, the EQE, M of the device can be certainly improved 1 ～M 3 Is three potential TADF molecules.
FIG. 10 shows the form M 4 ～M 6 The doping ratio of the light emitting layer dopant is 1wt%, 3wt% and 5wt% of the EQE of the device. M is M 4 ～M 6 M in molecule 5 The best EQE is shown. Overall M 1 ～M 3 The device exhibits lower external quantum efficiency at 10wt%, 15wt%, 20wt% doping. They exist with M 1 ～M 3 The same problem arises. If the two problems can be improved, the EQE, M of the device can be certainly improved 4 ～M 6 Is three potential TADF molecules.
The foregoing is merely a preferred embodiment of the application, and it should be noted that modifications and adaptations to those skilled in the art may be made without departing from the principles of the present application, which are intended to be comprehended within the scope of the present application.

Claims (3)

1. A thermally-activated delayed fluorescence molecular material based on indole fused ring units, characterized in that said material is selected from one of the following compounds:
2. use of a thermally active delayed fluorescence molecular material based on indole fused ring units as claimed in claim 1 as doping material for organic light emitting layers in electroluminescent devices.
3. An electroluminescent device, characterized in that: the organic light-emitting layer of the electroluminescent device is made of the indole fused ring unit-based thermally active delayed fluorescence molecular material of claim 1.
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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101874021A (en) * 2007-11-30 2010-10-27 出光兴产株式会社 Azaindenofluorenedione derivative, material for organic electroluminescent device, and organic electroluminescent device
CN102239140A (en) * 2008-12-03 2011-11-09 出光兴产株式会社 Indenofluorenedione derivative, material for organic electroluminescent element, and organic electroluminescent element
WO2017069208A1 (en) * 2015-10-20 2017-04-27 出光興産株式会社 Organic electroluminescent element
CN110615783A (en) * 2019-09-23 2019-12-27 大连理工大学 Electroluminescent material with pyrazinoindenone as electron acceptor and application thereof
CN111454251A (en) * 2020-04-10 2020-07-28 西安瑞联新材料股份有限公司 Pyrazine derivative and application thereof in O L ED device
CN113149864A (en) * 2020-12-29 2021-07-23 安徽秀朗新材料科技有限公司 Synthesis and application of thermal activity delayed fluorescent material based on indeno [2,1-a ] indene fused ring unit

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101874021A (en) * 2007-11-30 2010-10-27 出光兴产株式会社 Azaindenofluorenedione derivative, material for organic electroluminescent device, and organic electroluminescent device
CN102239140A (en) * 2008-12-03 2011-11-09 出光兴产株式会社 Indenofluorenedione derivative, material for organic electroluminescent element, and organic electroluminescent element
WO2017069208A1 (en) * 2015-10-20 2017-04-27 出光興産株式会社 Organic electroluminescent element
CN110615783A (en) * 2019-09-23 2019-12-27 大连理工大学 Electroluminescent material with pyrazinoindenone as electron acceptor and application thereof
CN111454251A (en) * 2020-04-10 2020-07-28 西安瑞联新材料股份有限公司 Pyrazine derivative and application thereof in O L ED device
CN113149864A (en) * 2020-12-29 2021-07-23 安徽秀朗新材料科技有限公司 Synthesis and application of thermal activity delayed fluorescent material based on indeno [2,1-a ] indene fused ring unit

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